HU219169B - Enzimet és késleltetett peroxisav fehérítő rendszert tartalmazó mosószer és alkalmazása - Google Patents

Enzimet és késleltetett peroxisav fehérítő rendszert tartalmazó mosószer és alkalmazása Download PDF

Info

Publication number: HU219169B
Authority: HU; Hungary
Prior art keywords: detergent composition; peroxyacid; acid; group; alkyl
Prior art date: 1994-04-13

Application number

HU9602815A

Other languages

English (en)

Hungarian (hu)

Other versions

HUT76032A (en

HU9602815D0 (en

Inventor

Gerard Marcel Baillely

Gail Margaret Baston

Janice Jeffrey

John Scott Park

Original Assignee

The Procter & Gamble Co.

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1994-04-13

Filing date

1995-03-24

Publication date

2001-02-28

1995-03-24 Application filed by The Procter & Gamble Co. filed Critical The Procter & Gamble Co.

1996-12-30 Publication of HU9602815D0 publication Critical patent/HU9602815D0/hu

1997-06-30 Publication of HUT76032A publication Critical patent/HUT76032A/hu

2001-02-28 Publication of HU219169B publication Critical patent/HU219169B/hu

Links

239000003599 detergent Substances 0.000 title claims abstract description 102
102000004190 Enzymes Human genes 0.000 title claims abstract description 62
108090000790 Enzymes Proteins 0.000 title claims abstract description 62
238000004061 bleaching Methods 0.000 title claims abstract description 27
150000004965 peroxy acids Chemical class 0.000 title claims description 36
230000003111 delayed effect Effects 0.000 title description 15
239000000203 mixture Substances 0.000 claims abstract description 179
150000001875 compounds Chemical class 0.000 claims abstract description 97
239000007844 bleaching agent Substances 0.000 claims abstract description 74
239000002243 precursor Substances 0.000 claims abstract description 63
229940088598 enzyme Drugs 0.000 claims abstract description 61
150000004967 organic peroxy acids Chemical class 0.000 claims abstract description 42
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 41
108090001060 Lipase Proteins 0.000 claims abstract description 14
239000004367 Lipase Substances 0.000 claims abstract description 14
102000004882 Lipase Human genes 0.000 claims abstract description 14
235000019421 lipase Nutrition 0.000 claims abstract description 14
108010065511 Amylases Proteins 0.000 claims abstract description 13
102000013142 Amylases Human genes 0.000 claims abstract description 13
108091005804 Peptidases Proteins 0.000 claims abstract description 11
235000019418 amylase Nutrition 0.000 claims abstract description 11
239000004365 Protease Substances 0.000 claims abstract description 8
229940025131 amylases Drugs 0.000 claims abstract description 6
108010084185 Cellulases Proteins 0.000 claims abstract description 4
102000005575 Cellulases Human genes 0.000 claims abstract description 4
108700020962 Peroxidase Proteins 0.000 claims abstract description 4
102000003992 Peroxidases Human genes 0.000 claims abstract description 4
102000035195 Peptidases Human genes 0.000 claims abstract description 3
108010059820 Polygalacturonase Proteins 0.000 claims abstract description 3
108010005774 beta-Galactosidase Proteins 0.000 claims abstract description 3
102000005936 beta-Galactosidase Human genes 0.000 claims abstract description 3
108010093305 exopolygalacturonase Proteins 0.000 claims abstract description 3
-1 cationic peroxyacid Chemical class 0.000 claims description 112
125000000217 alkyl group Chemical group 0.000 claims description 51
238000000034 method Methods 0.000 claims description 50
125000004432 carbon atom Chemical group C* 0.000 claims description 45
239000000243 solution Substances 0.000 claims description 45
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238000005406 washing Methods 0.000 claims description 37
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125000003118 aryl group Chemical group 0.000 claims description 25
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239000003446 ligand Substances 0.000 claims description 21
YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 claims description 13
229910052783 alkali metal Inorganic materials 0.000 claims description 13
125000002877 alkyl aryl group Chemical group 0.000 claims description 13
FRPJTGXMTIIFIT-UHFFFAOYSA-N tetraacetylethylenediamine Chemical compound CC(=O)C(N)(C(C)=O)C(N)(C(C)=O)C(C)=O FRPJTGXMTIIFIT-UHFFFAOYSA-N 0.000 claims description 13
239000000460 chlorine Substances 0.000 claims description 10
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MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical compound [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 claims description 10
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
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150000001340 alkali metals Chemical group 0.000 claims description 7
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125000003545 alkoxy group Chemical group 0.000 claims description 4
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125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims description 2
239000007983 Tris buffer Substances 0.000 claims description 2
125000004171 alkoxy aryl group Chemical group 0.000 claims description 2
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125000003710 aryl alkyl group Chemical group 0.000 claims description 2
LTKUVFYAHDCFPT-UHFFFAOYSA-L cobalt(2+) N-pyridin-2-ylpyridin-2-amine diperchlorate Chemical compound [Co++].[O-][Cl](=O)(=O)=O.[O-][Cl](=O)(=O)=O.N(c1ccccn1)c1ccccn1.N(c1ccccn1)c1ccccn1.N(c1ccccn1)c1ccccn1 LTKUVFYAHDCFPT-UHFFFAOYSA-L 0.000 claims description 2
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WLDGDTPNAKWAIR-UHFFFAOYSA-N 1,4,7-trimethyl-1,4,7-triazonane Chemical compound CN1CCN(C)CCN(C)CC1 WLDGDTPNAKWAIR-UHFFFAOYSA-N 0.000 claims 3
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HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 8
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150000004676 glycans Chemical class 0.000 description 1
BEBCJVAWIBVWNZ-UHFFFAOYSA-N glycinamide Chemical compound NCC(N)=O BEBCJVAWIBVWNZ-UHFFFAOYSA-N 0.000 description 1
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JEGIFBGJZPYMJS-UHFFFAOYSA-N imidazol-1-yl(phenyl)methanone Chemical compound C1=CN=CN1C(=O)C1=CC=CC=C1 JEGIFBGJZPYMJS-UHFFFAOYSA-N 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
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238000010348 incorporation Methods 0.000 description 1
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239000000976 ink Substances 0.000 description 1
150000002484 inorganic compounds Chemical class 0.000 description 1
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CDAISMWEOUEBRE-GPIVLXJGSA-N inositol Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O)[C@@H]1O CDAISMWEOUEBRE-GPIVLXJGSA-N 0.000 description 1
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230000003993 interaction Effects 0.000 description 1
SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical class OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
235000008960 ketchup Nutrition 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
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229910052919 magnesium silicate Inorganic materials 0.000 description 1
235000019792 magnesium silicate Nutrition 0.000 description 1
239000011565 manganese chloride Substances 0.000 description 1
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JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical group COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 description 1
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DZJFABDVWIPEIM-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)dodecan-1-amine oxide Chemical compound CCCCCCCCCCCC[N+]([O-])(CCO)CCO DZJFABDVWIPEIM-UHFFFAOYSA-N 0.000 description 1
IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 1
VMESOKCXSYNAKD-UHFFFAOYSA-N n,n-dimethylhydroxylamine Chemical class CN(C)O VMESOKCXSYNAKD-UHFFFAOYSA-N 0.000 description 1
UTTVXKGNTWZECK-UHFFFAOYSA-N n,n-dimethyloctadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)[O-] UTTVXKGNTWZECK-UHFFFAOYSA-N 0.000 description 1
RSVIRMFSJVHWJV-UHFFFAOYSA-N n,n-dimethyloctan-1-amine oxide Chemical compound CCCCCCCC[N+](C)(C)[O-] RSVIRMFSJVHWJV-UHFFFAOYSA-N 0.000 description 1
SKVFQANNTIZUQZ-UHFFFAOYSA-N n-[2-[bis[hydroxy(methoxy)phosphoryl]amino]ethyl]-n-[hydroxy(methoxy)phosphoryl]-methoxyphosphonamidic acid Chemical compound COP(O)(=O)N(P(O)(=O)OC)CCN(P(O)(=O)OC)P(O)(=O)OC SKVFQANNTIZUQZ-UHFFFAOYSA-N 0.000 description 1
WNGXRJQKUYDBDP-UHFFFAOYSA-N n-ethyl-n-methylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)([O-])CC WNGXRJQKUYDBDP-UHFFFAOYSA-N 0.000 description 1
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JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
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239000003960 organic solvent Substances 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
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239000000137 peptide hydrolase inhibitor Substances 0.000 description 1
239000002304 perfume Substances 0.000 description 1
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JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
125000005342 perphosphate group Chemical group 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
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229940068041 phytic acid Drugs 0.000 description 1
239000000467 phytic acid Substances 0.000 description 1
229920001983 poloxamer Polymers 0.000 description 1
229920000075 poly(4-vinylpyridine) Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
108010064470 polyaspartate Proteins 0.000 description 1
229920001748 polybutylene Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229910052573 porcelain Inorganic materials 0.000 description 1
229910001414 potassium ion Inorganic materials 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
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239000011164 primary particle Substances 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
NJKRDXUWFBJCDI-UHFFFAOYSA-N propane-1,1,2,3-tetracarboxylic acid Chemical class OC(=O)CC(C(O)=O)C(C(O)=O)C(O)=O NJKRDXUWFBJCDI-UHFFFAOYSA-N 0.000 description 1
NJEVMKZODGWUQT-UHFFFAOYSA-N propane-1,1,3,3-tetracarboxylic acid Chemical class OC(=O)C(C(O)=O)CC(C(O)=O)C(O)=O NJEVMKZODGWUQT-UHFFFAOYSA-N 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
230000002797 proteolythic effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000011403 purification operation Methods 0.000 description 1
PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
150000004023 quaternary phosphonium compounds Chemical class 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000006722 reduction reaction Methods 0.000 description 1
238000006268 reductive amination reaction Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
229960001860 salicylate Drugs 0.000 description 1
238000005464 sample preparation method Methods 0.000 description 1
235000015067 sauces Nutrition 0.000 description 1
CDAISMWEOUEBRE-UHFFFAOYSA-N scyllo-inosotol Natural products OC1C(O)C(O)C(O)C(O)C1O CDAISMWEOUEBRE-UHFFFAOYSA-N 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
229940071207 sesquicarbonate Drugs 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
229920002050 silicone resin Polymers 0.000 description 1
239000001509 sodium citrate Substances 0.000 description 1
229910001415 sodium ion Inorganic materials 0.000 description 1
235000019795 sodium metasilicate Nutrition 0.000 description 1
229910000031 sodium sesquicarbonate Inorganic materials 0.000 description 1
235000018341 sodium sesquicarbonate Nutrition 0.000 description 1
ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 description 1
RPQSWSMNPBZEHT-UHFFFAOYSA-M sodium;2-acetyloxybenzenesulfonate Chemical compound [Na+].CC(=O)OC1=CC=CC=C1S([O-])(=O)=O RPQSWSMNPBZEHT-UHFFFAOYSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000013042 solid detergent Substances 0.000 description 1
239000012265 solid product Substances 0.000 description 1
230000003381 solubilizing effect Effects 0.000 description 1
239000002195 soluble material Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
235000014347 soups Nutrition 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
125000000547 substituted alkyl group Chemical group 0.000 description 1
150000003890 succinate salts Chemical class 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
150000004026 tertiary sulfonium compounds Chemical class 0.000 description 1
238000004154 testing of material Methods 0.000 description 1
DCQJDRNKCUQEMA-UHFFFAOYSA-N tetradecanediperoxoic acid Chemical compound OOC(=O)CCCCCCCCCCCCC(=O)OO DCQJDRNKCUQEMA-UHFFFAOYSA-N 0.000 description 1
150000004685 tetrahydrates Chemical class 0.000 description 1
DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
125000004665 trialkylsilyl group Chemical group 0.000 description 1
QQOWHRYOXYEMTL-UHFFFAOYSA-N triazin-4-amine Chemical class N=C1C=CN=NN1 QQOWHRYOXYEMTL-UHFFFAOYSA-N 0.000 description 1
150000003852 triazoles Chemical group 0.000 description 1
PQDJYEQOELDLCP-UHFFFAOYSA-N trimethylsilane Chemical compound C[SiH](C)C PQDJYEQOELDLCP-UHFFFAOYSA-N 0.000 description 1
LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
229940038773 trisodium citrate Drugs 0.000 description 1
WCTAGTRAWPDFQO-UHFFFAOYSA-K trisodium;hydrogen carbonate;carbonate Chemical compound [Na+].[Na+].[Na+].OC([O-])=O.[O-]C([O-])=O WCTAGTRAWPDFQO-UHFFFAOYSA-K 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000001993 wax Substances 0.000 description 1
230000002087 whitening effect Effects 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/0039—Coated compositions or coated components in the compositions, (micro)capsules
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3907—Organic compounds
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3932—Inorganic compounds or complexes
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3935—Bleach activators or bleach catalysts granulated, coated or protected
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3942—Inorganic per-compounds
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3945—Organic per-compounds

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Oil, Petroleum & Natural Gas (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Inorganic Chemistry (AREA)
Detergent Compositions (AREA)

HU9602815A 1994-04-13 1995-03-24 Enzimet és késleltetett peroxisav fehérítő rendszert tartalmazó mosószer és alkalmazása HU219169B (hu)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB9407533A GB9407533D0 (en)	1994-04-13	1994-04-13	Detergent compositions
PCT/US1995/003707 WO1995028467A1 (fr)	1994-04-13	1995-03-24	Detergents contenant une enzyme et un systeme de peroxyacide de blanchiment a liberation retardee

Publications (3)

Publication Number	Publication Date
HU9602815D0 HU9602815D0 (en)	1996-12-30
HUT76032A HUT76032A (en)	1997-06-30
HU219169B true HU219169B (hu)	2001-02-28

Family

ID=10753617

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HU9602815A HU219169B (hu)	1994-04-13	1995-03-24	Enzimet és késleltetett peroxisav fehérítő rendszert tartalmazó mosószer és alkalmazása

Country Status (13)

Country	Link
EP (1)	EP0755432A4 (fr)
JP (1)	JPH09512047A (fr)
CN (1)	CN1083001C (fr)
AU (1)	AU2128095A (fr)
BR (1)	BR9507388A (fr)
CA (1)	CA2187303A1 (fr)
CZ (1)	CZ295596A3 (fr)
EG (1)	EG21025A (fr)
GB (1)	GB9407533D0 (fr)
HU (1)	HU219169B (fr)
MA (1)	MA23506A1 (fr)
PE (1)	PE50395A1 (fr)
WO (1)	WO1995028467A1 (fr)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9407279D0 (en) *	1994-04-13	1994-06-08	Procter & Gamble	Detergent compositions
AU4877296A (en) *	1995-02-18	1996-09-11	Albright & Wilson Uk Limited	Enzyme detergents
ATE300603T1 (de) †	1995-03-11	2005-08-15	Procter & Gamble	Wasch- und reinigungsmittel enthaltend wasserstoffperoxidquelle und protease
DE19600159A1 (de) *	1996-01-04	1997-07-10	Hoechst Ag	Bleichmittelsysteme enthaltend Bis- und Tris-(mu-oxo)-di-Mangan-Komplexsalze
AU738231B2 (en) *	1997-01-10	2001-09-13	Hinton, Elizabeth Jane	Detergent
DE19704634A1 (de)	1997-02-07	1998-08-27	Henkel Kgaa	pH-gesteuerte Freisetzung von Waschmittelkomponenten
GB9814968D0 (en) *	1998-07-10	1998-09-09	Hinton Gerald T	Detergent
EP2674475A1 (fr) *	2012-06-11	2013-12-18	The Procter & Gamble Company	Composition détergente
CA2921480A1 (fr)	2013-08-16	2015-02-19	Chemsenti Limited	Composition
EP4707372A2 (fr)	2018-06-15	2026-03-11	Ecolab USA Inc.	Stabilité améliorée du peroxygène à l'aide d'acide gras dans un solide peroxygéné contenant un agent d'activation de blanchiment
CN109971562A (zh) *	2019-04-23	2019-07-05	南京巨鲨显示科技有限公司	一种缓释型医用手工多酶清洗片及其制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4013575A (en) *	1975-11-28	1977-03-22	Fmc Corporation	Dry cleaning with peracids
IE51848B1 (en) *	1980-11-06	1987-04-15	Procter & Gamble	Bleach activator compositions,preparation thereof and use in granular detergent compositions
US4421664A (en) *	1982-06-18	1983-12-20	Economics Laboratory, Inc.	Compatible enzyme and oxidant bleaches containing cleaning composition
US4634551A (en) *	1985-06-03	1987-01-06	Procter & Gamble Company	Bleaching compounds and compositions comprising fatty peroxyacids salts thereof and precursors therefor having amide moieties in the fatty chain
US5130044A (en) *	1987-10-30	1992-07-14	The Clorox Company	Delayed onset active oxygen bleach composition
GB8803114D0 (en) *	1988-02-11	1988-03-09	Bp Chem Int Ltd	Bleach activators in detergent compositions
GB8908416D0 (en) *	1989-04-13	1989-06-01	Unilever Plc	Bleach activation
GB9214890D0 (en) *	1992-07-14	1992-08-26	Procter & Gamble	Washing process
US5405412A (en) *	1994-04-13	1995-04-11	The Procter & Gamble Company	Bleaching compounds comprising N-acyl caprolactam and alkanoyloxybenzene sulfonate bleach activators

1994
- 1994-04-13 GB GB9407533A patent/GB9407533D0/en active Pending
1995
- 1995-03-24 JP JP7526971A patent/JPH09512047A/ja not_active Ceased
- 1995-03-24 CZ CZ962955A patent/CZ295596A3/cs unknown
- 1995-03-24 HU HU9602815A patent/HU219169B/hu not_active IP Right Cessation
- 1995-03-24 WO PCT/US1995/003707 patent/WO1995028467A1/fr not_active Ceased
- 1995-03-24 EP EP95914180A patent/EP0755432A4/fr not_active Ceased
- 1995-03-24 BR BR9507388-4A patent/BR9507388A/pt not_active Application Discontinuation
- 1995-03-24 AU AU21280/95A patent/AU2128095A/en not_active Abandoned
- 1995-03-24 CA CA002187303A patent/CA2187303A1/fr not_active Abandoned
- 1995-03-24 CN CN95193554A patent/CN1083001C/zh not_active Expired - Fee Related
- 1995-04-12 EG EG29995A patent/EG21025A/xx active
- 1995-04-12 MA MA23834A patent/MA23506A1/fr unknown
- 1995-04-17 PE PE1995266501A patent/PE50395A1/es not_active Application Discontinuation

Also Published As

Publication number	Publication date
CN1150455A (zh)	1997-05-21
EP0755432A4 (fr)	1998-12-16
PE50395A1 (es)	1996-02-14
AU2128095A (en)	1995-11-10
MA23506A1 (fr)	1995-12-31
BR9507388A (pt)	2002-04-16
WO1995028467A1 (fr)	1995-10-26
HUT76032A (en)	1997-06-30
GB9407533D0 (en)	1994-06-08
EG21025A (en)	2000-09-30
CN1083001C (zh)	2002-04-17
JPH09512047A (ja)	1997-12-02
CA2187303A1 (fr)	1995-10-26
CZ295596A3 (en)	1997-04-16
HU9602815D0 (en)	1996-12-30
EP0755432A1 (fr)	1997-01-29

Legal Events

Date	Code	Title	Description
2004-12-28	HMM4	Cancellation of final prot. due to non-payment of fee

Publication	Publication Date	Title
JP4393582B2 (ja)	2010-01-06	重金属封鎖剤および遅延放出ペルオキシ酸漂白剤系を含む洗剤
US5965505A (en)	1999-10-12	Detergents containing a heavy metal sequestrant and a delayed release peroxyacid bleach system
US6046149A (en)	2000-04-04	Detergent compositions
MXPA98000274A (en)	1998-04-01	Washing method of r
US5755992A (en)	1998-05-26	Detergents containing a surfactant and a delayed release peroxyacid bleach system
HUT77961A (hu)	1998-12-28	Mosodai mosási eljárás egy szilárd fehérítő mosószer kibocsátására szolgáló eszköz alkalmazásával
EP0755434B1 (fr)	2005-03-16	Detergents contenant un adjuvant de lavage et une enzyme liberee avec un retard
HU219169B (hu)	2001-02-28	Enzimet és késleltetett peroxisav fehérítő rendszert tartalmazó mosószer és alkalmazása
EP0755435A1 (fr)	1997-01-29	Compositions detergentes
US6559113B2 (en)	2003-05-06	Detergents containing a builder and a delayed released enzyme
JP3174068B2 (ja)	2001-06-11	洗剤組成物
CA2187436C (fr)	2000-08-08	Detergents contenant un tensioactif et une source d'un agent de blanchiment du type peroxyacide libere avec un retard
CA2187306C (fr)	2000-05-30	Detergents contenant un tensioactif et une enzyme a liberation retardee
WO1997023593A1 (fr)	1997-07-03	Composition detergente comprenant une enzyme et un retardateur de liberation
JPH09512045A (ja)	1997-12-02	ビルダーおよび遅延放出ペルオキシ酸漂白剤供給源を含む洗剤
EP0861315B1 (fr)	2004-08-04	Detergents liberant dans une solution de lavage un agent de blanchiment au peroxyacide faible immediatement suivi par la liberation d'un peroxyacide fort
JPH09512044A (ja)	1997-12-02	洗剤組成物
HUT78045A (hu)	1999-07-28	Peroxid-forrást, fehérítő prekurzort és hidrogén-peroxid gyökfogót tartalmazó mosószerek és előállításuk
JPH09137196A (ja)	1997-05-27	漂白組成物
MXPA96004782A (en)	1998-01-01	Detergent compositions
MXPA96004814A (en)	1998-02-01	Detergents containing a detergency improver and a retard release enzyme
MXPA96004781A (en)	1998-01-01	Detergents containing an enzyme and a retard releasing peroxiacide sistemablanqueador